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Results 1 - 10 of 20 for Amyotrophic lateral sclerosis type 9
  1. C19orf12 gene 
    ... to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition ... with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis. J Neurol. 2012 Nov;259(11):2434-9. doi: 10.1007/s00415-012-6521-7. Epub ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics
  2. Amyotrophic lateral sclerosis 
    ... SCLEROSIS 7; ALS7 AMYOTROPHIC LATERAL SCLEROSIS 3; ALS3 AMYOTROPHIC LATERAL SCLEROSIS 9; ALS9 AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT ... LATERAL SCLEROSIS 20; ALS20 FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC ... 9; FTDALS9 FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
  3. FUS gene 
    ... in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science. 2009 Feb 27;323(5918):1208- ...
    https://medlineplus.gov/genetics/gene/fus - Genetics
  4. Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Living With ... Neuromuscular Disorders ... muscular dystrophy; exercise with a disability; neuromuscular disease; adapted exercise; accesible ...
    https://www.mda.org/.../files/MDA_Quest_Excercise_Package_2009.pdf - External Health Links
  5. Pregnancy and Childbirth with Neuromuscular Disease (Muscular Dystrophy Association) - PDF  
    Neuromuscular Disorders/Women ... Neuromuscular Disorders ... Muscular Dystrophy Association ... PDF
    https://www.mda.org/.../Quest17-3_Pregnancy_Series_revised_0.pdf - External Health Links
  6. C9orf72 gene 
    ... the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol. 2012 Apr;11(4):323-30. doi: 10.1016/S1474-4422(12)70043-1. Epub 2012 Mar 9. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  7. Charcot-Marie-Tooth disease 
    ... the nerve impulse. People with CMT2 may develop amyotrophic lateral sclerosis ... as intermediate type, the nerve impulses are both slowed and reduced ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  8. SETX gene 
    ... of damaged DNA. MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition At least 125 mutations in the SETX gene have been found to cause ataxia with oculomotor apraxia type 2. This condition is characterized by difficulty coordinating ...
    https://medlineplus.gov/genetics/gene/setx - Genetics
  9. SPG11 gene 
    ... cause the signs and symptoms of spastic paraplegia type 11 by interfering with the protein's ... This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  10. Vitamin E (Harvard School of Public Health)  
    Vitamin E/Learn More ... Vitamin E ... Harvard School of Public Health ... Vitamin E is a fat-soluble vitamin which acts as an antioxidant in the body. It also enhances ...
    https://www.hsph.harvard.edu/nutritionsource/vitamins/vitamin-e - External Health Links
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